| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23306605-23306911 | Common:1; Rare:67 | ||||
| chr14:23321817-23322074 | Common:2; Rare:75 | ||||
| chr14:23469649-23469727 | Rare:27 | ||||
| chr14:23555926-23556356 | Common:4; Rare:106 | ||||
| chr14:23567481-23567579 | Rare:28 | ||||
| chr14:23567737-23567906 | Rare:32 | ||||
| chr14:23953661-23953817 | Common:6; Rare:55 | ||||
| chr14:23954116-23954349 | Common:2; Rare:68 | ||||
| chr14:23969856-23970016 | Common:8; Rare:69 | ||||
| chr14:23988756-23988938 | Common:8; Rare:74 | ||||
| chr14:24094013-24094427 | Common:4; Rare:112; Clinvar (benign):1 | ||||
| chr14:24114468-24114864 | Common:1; Rare:94 | ||||
| chr14:24114934-24115302 | Common:2; Rare:109 | ||||
| chr14:24135910-24136301 | Common:1; Rare:122 | ||||
| chr14:24141442-24141874 | Common:2; Rare:107 |